Cytoprep Inc. Est.

Cytoprep Inc. Est. holds 1 FDA 510(k) medical device clearance, cleared in 1998.

Top product codes for Cytoprep Inc. Est.

HHI — Obstetrics/Gynecology1 device

Recent clearances by Cytoprep Inc. Est.

K983181 — CYTOPREPCode HHI·1998-11-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.